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Monoclonal Anti Sera -AB - India CDSCO Medical Device Registration

Monoclonal Anti Sera -AB is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000085_d4d645cae4afccb43cb216e7d3d46036_e740082ed52c00522632d7405047fa16. This device is marketed under the brand name Rapid Plasma Reagin. The license holder is Voxtur Bio Ltd, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class D
Monoclonal Anti Sera -AB
UID: MFG/IVD/2022/000085_d4d645cae4afccb43cb216e7d3d46036_e740082ed52c00522632d7405047fa16

Brand Name

Rapid Plasma Reagin

License Holder

Voxtur Bio Ltd

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Monoclonal Anti-AB for Qualitative determination of ABO Blood Grouping in Human Blood

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